Young Adult Education on Alcohol & Health
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Online program.
- Who it may be relevant to
- Registry conditions: Sexual Behavior, Alcohol Drinking, Condomless Sex. Basic parameters: 18 years — 24 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
A Technology-based Intervention for Alcohol-related Sexual Risk Behaviors in Young Women
Overview
The goal of this clinical trial is to test the effectiveness of our brief online program when compared to those who don't complete the program at all.
Detailed description
A total of 300 participants will complete this 6 month study. The study will include a background survey, 5 week monitoring period where participants either complete the brief online program with check-in surveys or check-in surveys only, and follow-up surveys 1, 3, and 6 months later.
Interventions
- Behavioral Online program
The online program is 4 weeks and focused on topics such as alcohol and sexual health
Primary outcome measures
- Drinking before sex (frequency) [Time frame: Follow up (1 month, 3 month, 6 months)]
- Drinking before sex (quantity) [Time frame: Follow up (1 month, 3 month, 6 months)]
- Condomless sex [Time frame: Follow up (1 month, 3 month, 6 months)]
Eligibility criteria
Inclusion criteria
- Assessed as part of screening procedures
Exclusion criteria
- Do not want to participate
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Prevention
Study locations
United States · 1 center
- University of Washington — Seattle
Identifiers
NCT: NCT05620849 · STUDY00010940 · 1K99AA028777-01 · 4R00AA028777